Similar articles for PMID: 35114785

Year	Number of Results
2005	1
2007	6
2008	3
2009	5
2010	6
2011	7
2012	9
2013	8
2014	4
2015	7
2016	8
2017	11
2018	6
2019	4
2020	10
2021	13
2022	3
2023	1
2024	0

1

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt.

Abdelmeguid Y, Mowafy EW, Marzouk I, Franco E, ElSayed S. Abdelmeguid Y, et al. Ann Pediatr Endocrinol Metab. 2022 Sep;27(3):214-222. doi: 10.6065/apem.2142184.092. Epub 2022 Jan 26. Ann Pediatr Endocrinol Metab. 2022. PMID: 35114785 Free PMC article.

2

Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience.

Abali ZY, De Franco E, Karakilic Ozturan E, Poyrazoglu S, Bundak R, Bas F, Flanagan SE, Darendeliler F. Abali ZY, et al. Horm Res Paediatr. 2020;93(7-8):423-432. doi: 10.1159/000512247. Epub 2021 Jan 26. Horm Res Paediatr. 2020. PMID: 33498041 Free PMC article.

3

Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K_ATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.

Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC. Ngoc CTB, et al. Front Endocrinol (Lausanne). 2021 Sep 9;12:727083. doi: 10.3389/fendo.2021.727083. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34566892 Free PMC article.

4

Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey.

Denkboy Öngen Y, Eren E, Demirbaş Ö, Sobu E, Ellard S, De Franco E, Tarım Ö. Denkboy Öngen Y, et al. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):80-87. doi: 10.4274/jcrpe.galenos.2020.2020.0093. Epub 2020 Aug 21. J Clin Res Pediatr Endocrinol. 2021. PMID: 32820876 Free PMC article.

5

Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience.

Laimon W, El-Ziny M, El-Hawary A, Elsharkawy A, Salem NA, Aboelenin HM, Awad MH, Flanagan SE, De Franco E. Laimon W, et al. Acta Diabetol. 2021 Dec;58(12):1689-1700. doi: 10.1007/s00592-021-01788-6. Epub 2021 Aug 23. Acta Diabetol. 2021. PMID: 34426871

6

Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes.

Asl SN, Vakili R, Vakili S, Soheilipour F, Hashemipour M, Ghahramani S, De Franco E, Yaghootkar H. Asl SN, et al. J Pediatr Endocrinol Metab. 2019 Jun 26;32(6):607-613. doi: 10.1515/jpem-2018-0434. J Pediatr Endocrinol Metab. 2019. PMID: 31141482

7

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.

Demirbilek H, Arya VB, Ozbek MN, Houghton JA, Baran RT, Akar M, Tekes S, Tuzun H, Mackay DJ, Flanagan SE, Hattersley AT, Ellard S, Hussain K. Demirbilek H, et al. Eur J Endocrinol. 2015 Jun;172(6):697-705. doi: 10.1530/EJE-14-0852. Epub 2015 Mar 9. Eur J Endocrinol. 2015. PMID: 25755231 Free PMC article.

8

Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.

Alkorta-Aranburu G, Carmody D, Cheng YW, Nelakuditi V, Ma L, Dickens JT, Das S, Greeley SAW, Del Gaudio D. Alkorta-Aranburu G, et al. Mol Genet Metab. 2014 Dec;113(4):315-320. doi: 10.1016/j.ymgme.2014.09.007. Epub 2014 Sep 28. Mol Genet Metab. 2014. PMID: 25306193 Free PMC article.

9

Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates.

Deeb A, Habeb A, Kaplan W, Attia S, Hadi S, Osman A, Al-Jubeh J, Flanagan S, DeFranco E, Ellard S. Deeb A, et al. Am J Med Genet A. 2016 Mar;170(3):602-9. doi: 10.1002/ajmg.a.37419. Epub 2015 Oct 13. Am J Med Genet A. 2016. PMID: 26463504

10

Neonatal Diabetes Mellitus: Novel Mutations.

Nayak S, Sarangi AN, Sahoo SK, Mangla P, Tripathy M, Rao S, Gupta S, Paliwal VK, Sudhanshu S, Ravi C, Joshi K, Bhatia V, Bhatia E. Nayak S, et al. Indian J Pediatr. 2021 Aug;88(8):785-792. doi: 10.1007/s12098-020-03567-7. Epub 2021 Jan 7. Indian J Pediatr. 2021. PMID: 33409956

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